Format

Send to

Choose Destination
Am J Hematol. 2018 Dec 21. doi: 10.1002/ajh.25385. [Epub ahead of print]

IGH translocations in chronic lymphocytic leukemia: Clinicopathologic features and clinical outcomes.

Author information

1
Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
2
Division of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
3
Division of Hematology, Mayo Clinic, Rochester, Minnesota.
4
Division of Hematology and Oncology, Mayo Clinic, Phoenix, Arizona.
5
Division of Hematology and Oncology, Mayo Clinic, Jacksonville, Florida.
6
Division of Laboratory Genetics, Mayo Clinic, Rochester, Minnesota.
7
Division of Hematology, Stanford Medicine, Palo Alto, California.

Abstract

The prevalence, clinicopathologic correlates, and outcomes of previously untreated chronic lymphocytic leukemia (CLL) patients with IGH-BCL2 and IGH-BCL3 translocations are not well known. Using the Mayo Clinic CLL database, we identified patients seen between March 1, 2002 and September 30, 2016 who had FISH testing performed within 3 years of CLL diagnosis. The prognostic profile, time to first therapy (TTT), and overall survival (OS) of patients with IGH-BCL2 and IGH-BCL3 translocation were compared to patients without these abnormalities (non-IGH group). Of 1684 patients who met the inclusion criteria, 38 (2.2%) had IGH-BCL2, and 16 (0.9%) had IGH-BCL3 translocation at diagnosis. Patients with IGH-BCL3 translocation were more likely to have high and very-high CLL-International Prognostic Index, compared to patients with IGH-BCL2 translocation and the non-IGH group. The 5-year probability of requiring therapy was significantly higher for IGH-BCL3 compared to IGH-BCL2 and non-IGH groups (84% vs 33% vs 29%, respectively, P < 0.0001). The 5-year OS was significantly shorter for IGH-BCL3 compared to IGH-BCL2 and non-IGH groups (45% vs 89% vs 86%, respectively, P < 0.0001). On multivariable analyses, IGH-BCL3 translocation was associated with a shorter TTT (hazard ratio [HR] = 2.7; P = 0.005) and shorter OS (HR = 5.5; P < 0.0001); IGH-BCL2 translocation did not impact TTT and OS. In conclusion, approximately 3% of all newly diagnosed CLL patients have either an IGH-BCL2 or IGH-BCL3 translocation. Patients with IGH-BCL3 translocations have a distinct prognostic profile and outcome. These results support the inclusion of an IGH probe during the routine evaluation of FISH abnormalities in newly diagnosed CLL.

PMID:
30575108
DOI:
10.1002/ajh.25385

Supplemental Content

Loading ...
Support Center